Canonical Allele Identifier: CA915943077

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78369906del , CM000666.2:g.78369906del	GRCh38
NC_000004.11:g.79291060del , CM000666.1:g.79291060del	GRCh37
NC_000004.10:g.79510084del	NCBI36
NG_015812.1:g.317337del
NG_015812.2:g.317337del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325942.11:c.2791del	ENSP00000326330.6:p.Val931PhefsTer?
ENST00000682513.1:c.2791del	ENSP00000508201.1:p.Val931PhefsTer?
ENST00000684159.1:c.2791del	ENSP00000506875.1:p.Val931PhefsTer?
ENST00000512123.4:c.2791del MANE Select	ENSP00000422834.2:p.Val931PhefsTer?
ENST00000264899.10:c.845-74197del	ENSP00000264899.7:n.845-74197del
ENST00000325942.10:c.2791del	ENSP00000326330.6:p.Val931PhefsTer?
ENST00000512123.3:c.2791del	ENSP00000422834.2:p.Val931PhefsTer?
NM_001166133.1:c.2791del	NP_001159605.1:p.Val931PhefsTer?
NM_025074.6:c.2791del	NP_079350.5:p.Val931PhefsTer?
XM_006714314.1:c.2791del	XP_006714377.1:p.Val931PhefsTer?
XM_006714316.1:c.2791del	XP_006714379.1:p.Val931PhefsTer?
XM_011532270.1:c.490del	XP_011530572.1:p.Val164PhefsTer?
XM_006714316.3:c.2791del	XP_006714379.1:p.Val931PhefsTer?
NM_025074.7:c.2791del MANE Select	NP_079350.5:p.Val931PhefsTer?
NM_001166133.2:c.2791del	NP_001159605.1:p.Val931PhefsTer?